US10714224B2 - Method of preparing of irradiation targets for radioisotope production and irradiation target - Google Patents
Method of preparing of irradiation targets for radioisotope production and irradiation target Download PDFInfo
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- US10714224B2 US10714224B2 US15/545,807 US201515545807A US10714224B2 US 10714224 B2 US10714224 B2 US 10714224B2 US 201515545807 A US201515545807 A US 201515545807A US 10714224 B2 US10714224 B2 US 10714224B2
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- rare earth
- earth metal
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- metal oxide
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- 238000000034 method Methods 0.000 title claims abstract description 48
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 239000000843 powder Substances 0.000 claims abstract description 41
- 229910001404 rare earth metal oxide Inorganic materials 0.000 claims abstract description 37
- 238000005245 sintering Methods 0.000 claims abstract description 32
- 239000011230 binding agent Substances 0.000 claims abstract description 28
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 12
- 150000002910 rare earth metals Chemical class 0.000 claims abstract description 11
- 238000005453 pelletization Methods 0.000 claims abstract description 9
- 239000007790 solid phase Substances 0.000 claims abstract description 5
- 230000004907 flux Effects 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 229910052689 Holmium Inorganic materials 0.000 claims description 5
- 229910052727 yttrium Inorganic materials 0.000 claims description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 4
- 229910052772 Samarium Inorganic materials 0.000 claims description 4
- 229910052769 Ytterbium Inorganic materials 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 4
- 229910052692 Dysprosium Inorganic materials 0.000 claims description 3
- 229910052691 Erbium Inorganic materials 0.000 claims description 3
- 229910052765 Lutetium Inorganic materials 0.000 claims description 3
- 229910052775 Thulium Inorganic materials 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 229910052779 Neodymium Inorganic materials 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229920000609 methyl cellulose Polymers 0.000 claims description 2
- 239000001923 methylcellulose Substances 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 238000005054 agglomeration Methods 0.000 description 7
- 230000002776 aggregation Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 239000012535 impurity Substances 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 238000005238 degreasing Methods 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- FIXNOXLJNSSSLJ-UHFFFAOYSA-N ytterbium(III) oxide Inorganic materials O=[Yb]O[Yb]=O FIXNOXLJNSSSLJ-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000002059 diagnostic imaging Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 238000011275 oncology therapy Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000013077 target material Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- NLQFUUYNQFMIJW-UHFFFAOYSA-N dysprosium(III) oxide Inorganic materials O=[Dy]O[Dy]=O NLQFUUYNQFMIJW-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- VQCBHWLJZDBHOS-UHFFFAOYSA-N erbium(III) oxide Inorganic materials O=[Er]O[Er]=O VQCBHWLJZDBHOS-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- JYTUFVYWTIKZGR-UHFFFAOYSA-N holmium oxide Inorganic materials [O][Ho]O[Ho][O] JYTUFVYWTIKZGR-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910003443 lutetium oxide Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- ZIKATJAYWZUJPY-UHFFFAOYSA-N thulium (III) oxide Inorganic materials [O-2].[O-2].[O-2].[Tm+3].[Tm+3] ZIKATJAYWZUJPY-UHFFFAOYSA-N 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21G—CONVERSION OF CHEMICAL ELEMENTS; RADIOACTIVE SOURCES
- G21G1/00—Arrangements for converting chemical elements by electromagnetic radiation, corpuscular radiation or particle bombardment, e.g. producing radioactive isotopes
- G21G1/02—Arrangements for converting chemical elements by electromagnetic radiation, corpuscular radiation or particle bombardment, e.g. producing radioactive isotopes in nuclear reactors
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05H—PLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
- H05H6/00—Targets for producing nuclear reactions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E30/00—Energy generation of nuclear origin
- Y02E30/30—Nuclear fission reactors
Definitions
- the present invention is directed to a method for preparing irradiation targets used to produce radioisotopes in the instrumentation tubes of a nuclear power reactor, and an irradiation target obtained by this method.
- Radioisotopes find applications various fields such as industry, research, agriculture and medicine. Artificial radioisotopes are typically produced by exposing a suitable target material to neutron flux in a cyclotron or in a nuclear research reactor for an appropriate time. Irradiation sites in nuclear research reactors are expensive and will become even more scarce in future due to the age-related shut-down of reactors.
- EP 2 093 773 A2 is directed to a method of producing radioisotopes using the instrumentation tubes of a commercial nuclear power reactor, the method comprising: choosing at least one irradiation target with a known neutron cross-section; inserting the irradiation target into an instrumentation tube of a nuclear reactor, the instrumentation tube extending into the reactor and having an opening accessible from an exterior of the reactor, to expose the irradiation target to neutron flux encountered in the nuclear reactor when operating, the irradiation target substantially converting to a radioisotope when exposed to a neutron flux encountered in the nuclear reactor, wherein the inserting includes positioning the irradiation target at an axial position in the instrumentation tube for an amount of time corresponding to an amount of time required to convert substantially all the irradiation target to a radioisotope at a flux level corresponding to the axial position based on an axial neutron flux profile of the operating nuclear reactor; and removing the irradiation target and produced radioisotop
- the roughly spherical irradiation targets may be generally hollow and include a liquid, gaseous and/or solid material that converts to a useful gaseous, liquid and/or solid radioisotope.
- the shell surrounding the target material may have negligible physical changes when exposed to a neutron flux.
- the irradiation targets may be generally solid and fabricated from a material that converts to a useful radioisotope when exposed to neutron flux present in an operating commercial nuclear reactor.
- the neutron flux density in the core of a commercial nuclear reactor is measured, inter alia, by introducing solid spherical probes of a ball measuring system into instrumentation tubes passing through the reactor core using pressurized air for driving the probes.
- solid spherical probes of a ball measuring system into instrumentation tubes passing through the reactor core using pressurized air for driving the probes.
- pressurized air for driving the probes.
- EP1 336 596 B1 discloses a transparent sintered rare earth metal oxide body represented by the general formula R 2 O 3 wherein R is at least one element of a group comprising Y, Dy, Ho, Er, Tm, Yb and Lu.
- the sintered body is prepared by providing a mixture of a binder and a high-purity rare earth metal oxide material powder having a purity of 99.9% or more, and having an Al content of 5-100 wtppm in metal weight and an Si content of 10 wtppm or less in metal weight, to prepare a molding body having a green density of 58% or more of the theoretical density.
- the binder is eliminated by thermal treatment, and the molding body is sintered in an hydrogen or inert gas atmosphere or in a vacuum at a temperature of between 1450° C. and 1700° C. for 0.5 hour or more.
- the addition of Al serves as a sintering aid and is carefully controlled so that the sintered body has a mean grain size of between 2 and 20 ⁇ m.
- U.S. Pat. No. 8,679,998 B2 discloses a corrosion-resistant member for use in a semiconductor manufacturing apparatus.
- An Yb 2 O 3 raw material having a purity of at least 99.9% is subjected to uniaxial pressure forming at a pressure of 200 kgf/cm 2 (19.6 MPa), so as to obtain a disc-shaped compact having a diameter of about 35 mm and a thickness of about 10 mm.
- the compact is placed into a graphite mold for firing. Firing is performed using a hot-press method at a temperature of 1800° C. under an Ar atmosphere for at least 4 hours to obtain a corrosion-resistant member for semiconductor manufacturing apparatus.
- the pressure during firing is 200 kgf/cm 2 (19.6 MPa).
- the Yb 2 O 3 sintered body has an open porosity of 0.2%.
- the above methods generally provide sintered rare earth metal oxide bodies adapted to specific applications such as corrosion-resistance or optical transparency.
- none of the sintered bodies produced by these methods has properties required for irradiation targets used for radioisotope production in commercial nuclear power reactors.
- Powder agglomeration techniques are known to a person skilled in the art for producing compacted spherical bodies.
- a rotating drum for powder agglomeration is disclosed, for example, in EP 0 887 102 A2.
- this object is solved by a method for the production of irradiation targets according to claim 1 .
- the irradiation targets obtained by the method of the present invention have small dimensions adapted for use in commercially existing ball measuring systems, and also fulfill the requirements with respect to pressure resistance, temperature resistance and shear resistance so that they are sufficiently stable when being inserted in a ball measuring system and transported through the reactor core by means of pressurized air.
- the targets can be provided with a smooth surface to avoid abrasion of the instrumentation tubes.
- the irradiation targets have a chemical purity which render them useful for radioisotope production.
- the invention provides a method of preparing irradiation targets for radioisotope production in instrumentation tubes of a nuclear power reactor, the method comprising the steps of:
- a powder consisting of an oxide of a rare earth metal having a purity of greater than 99% and, optionally, an organic binder;
- the invention resorts to processes known from the manufacture of sintered ceramics and can therefore be carried out on commercially available equipment, including appropriate pelletizing or granulating devices and sintering facilities.
- Powder agglomeration also allows for providing targets having a narrow particle size distribution of the pellets (granules) and a substantially spherical shape, which facilitate use in existing instrumentation tubes for ball measuring systems.
- the costs for preparing the irradiation targets can be kept low since mass production of suitable radioisotope precursor targets will be possible.
- the method is also variable and useful for producing many different targets having the required chemical purity.
- the sintered targets are found to be mechanically stable and in particular resistant to transportation within instrumentation tubes using pressurized air even at temperatures of up to 400° C. present in the nuclear reactor core.
- the oxide is represented by the general formula R 2 O 3 wherein R is a rare earth metal selected from the group consisting of Nd, Sm, Y, Dy, Ho, Er, Tm, Yb and Lu.
- the rare earth metal is Sm, Y, Ho, or Yb, preferably Yb-176 which is useful for producing Lu-177, or Yb-168 which can be used to produce Yb-169.
- TREO Total Rare Earth Oxide
- the inventors also contemplate that neutron capturing impurities such as B, Cd, Gd should be absent.
- the powder of the rare earth metal oxide has an average grain size in the range of between 5 and 50 ⁇ m.
- Oxide powders suitable for powder agglomeration are commercially available from ITM Isotopen Technologie Kunststoff AG.
- the powder is enriched of Yb-176 with a degree of enrichment of >99%.
- the powder of the rare earth metal oxide is pelletized by agglomerating in a rotating drum or on a pelletizing disc.
- an organic binder is added to the oxide powder during the pelletizing step, preferably by spraying an aqueous solution of the binder onto the powder. It is also possible to provide a powder mixture of an organic binder and the rare earth metal oxide, and subject the powder mixture to pelletizing by agglomeration in a rotating drum or on a pelletizing disc.
- the organic binder is an organic polymer, most preferably a polyvinyl alcohol or methylcellulose.
- the organic binder is used in an amount so that the green bodies have a binder content of up to 1 weight percent based on the total weight of the pelletized green bodies, preferably a binder content in a range of from 0.5 to 1 weight percent.
- the substantially spherical green bodies preferably have a diameter in a range of between 1 to 5 mm, more preferably from 1 to 3 mm. Most preferably, the size of the spherical green bodies is in a range of from 2 to 3 mm.
- substantially spherical means that the body is capable of rolling, but does not necessarily have the form of a perfect sphere.
- the rare earth metal oxide powder is pelletized by means of powder agglomeration to form the substantially spherical green body without the use of a binder.
- the oxide powder to be pelletized consists of the rare earth metal oxide having a purity of greater than 99%, preferably greater than 99.9 percent or greater than 99.99 percent.
- the rare earth metal oxide powder also does not contain any sintering aids.
- binders and/or sintering aids typically used for sintering of rare earth metal oxides may be a source of undesired impurities, but that use of these additives is not necessary, or can be reduced to an amount of 1 weight percent or less in the case of the organic binder, for obtaining a sintered rare earth metal oxide target having a sufficient density.
- the green density of the pelletized green body is at least 30 percent of the theoretical density, more preferably at least 40 percent and still more preferably in a range of from 30 to 50 percent of the theoretical density.
- the green density is sufficient to facilitate automated processing of the pelletized green body.
- the spherical green body may be polished to improve its sphericity or roundness.
- the green body is preferably kept at a sintering temperature of between 70 and 80 percent of the solidus temperature of the rare earth metal oxide. More preferably, the sintering temperature is in a range of between 1650 and 1800° C. The inventors found that a sintering temperature in this range is suitable for sintering most rare earth metal oxides to a high sintering density of at least 80 percent, preferably at least 90 percent of the theoretical density.
- the green body is kept at the sintering temperature and sintered for a time of from 4 to 24 hours, preferably under atmospheric pressure.
- the green body is sintered in an oxidizing atmosphere such as in a mixture of nitrogen and oxygen, preferably synthetic air.
- the green body can also be sintered in a reducing atmosphere such as a mixture consisting of nitrogen and hydrogen.
- the green bodies containing the organic binder Prior to sintering, can be subjected to a degreasing step, preferably by keeping the bodies at a temperature of about 800 to 1000° C. for a time sufficient to evaporate or decompose the organic binder.
- the degreasing step can also be part of the sintering step and be performed when heating the green bodies up to the sintering temperature.
- the sintered rare earth metal oxide target may be polished or ground to remove superficial residues and improve its surface roughness.
- This post-sintering treatment may reduce abrasion of the instrumentation tubes by the sintered targets when inserted at high pressure.
- the invention is directed to a sintered target obtained by the above described method, wherein the sintered target is substantially spherical and has a density of at least 80 percent of the theoretical density, and wherein the rare earth metal oxide has a purity of greater than 99%, preferably greater than 99.9 percent or greater than 99.99 percent.
- the sintered target has a density of at least 90 percent of the theoretical density, and a porosity of less than 10%.
- the density and therefore porosity can be determined by measuring in a pycnometer.
- the targets obtained by the method of the present invention are resistant to a pneumatic inlet pressure of 10 bar used in commercial ball measuring systems and an impact velocity of 10 m/s.
- the targets have been subjected to high sintering temperatures, it is understood that the sintered targets are capable to withstand processing temperatures in the order of about 400° C. present in the core of an operating nuclear reactor.
- the sintered rare earth metal oxide targets are used for producing one or more radioisotopes in an instrumentation tube of a nuclear power reactor when in energy producing operation.
- the sintered targets are inserted in an instrumentation tube extending into the reactor core by means of pressurized air, preferably at a pressure of about 7 to 30 bar, and are exposed to neutron flux encountered in the nuclear reactor when operating, for a predetermined period of time, so that the sintered target substantially converts to a radioisotope, and removing the sintered target and produced radioisotope from the instrumentation tube.
- a sintered ytterbia target was produced by providing an ytterbia powder, pelletzing the powder in a rotating drum to form a substantially spherical green body, and sintering the green body in solid phase to form a substantially spherical ytterbia target.
- the ytterbia powder had a purity of greater than 99%/TREO, with the following specification being used:
- the ytterbia powder was pelletized in a rotating drum by agglomerating the powder while spraying an aqueous solution of polyvinyl alcohol (5 weight percent PVA) onto the powder.
- Substantially spherical green bodies having a diameter of about 2.5 mm+/ ⁇ 0.3 mm were formed and harvested from the rotating drum.
- the green bodies had a density of about 4-5 cm 3 , corresponding to a green density of about 50 percent of the theoretical density.
- the substantially spherical ytterbia green bodies were subjected to a degreasing treatment at about 1000° C. for removing the organic binder, and sintered in solid phase by keeping them at a temperature of about 1700° C. for at least four hours under an atmosphere of synthetic air at atmospheric pressure.
- the ytterbia green bodies were placed in MgO saggers to avoid uptake of alumina from the sintering furnace.
- Sintered ytterbia targets of a substantially spherical shape were obtained having a diameter of about 1.5 to 2 mm and a sintered density of about 7.8 g/cm 3 , corresponding to about 85 percent of the theoretical density.
- the sintering atmosphere was varied from an oxidizing atmosphere consisting of synthetic air to a reducing atmosphere consisting of nitrogen and hydrogen.
- the sintered ytterbia targets obtained from sintering in reducing atmosphere had a dark colour indicating a change in the stoichiometric composition. Accordingly, use of a reducing sintering atmosphere is possible but less preferred.
- Ytterbia-176 is considered to be useful for producing the radioisotope Lu-177 which has applications in medical imaging and cancer therapy, but which cannot be stored over a long period of time due to its short half-life of about 6.7 days.
- Yb-176 is converted into Lu-177 according to the following reaction: 176 Yb ( n , ⁇ ) 177 Yb ( ⁇ , ⁇ ) 177 Lu.
- the sintered targets of ytterbia oxide obtained by the method of the present invention are useful precursors for the production of Lu-177 in the instrumentation tubes of a nuclear reactor during energy producing operation. Similar reactions are known to the person skilled in the art for the production of other radioisotopes from various rare earth oxide precursors.
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- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- High Energy & Nuclear Physics (AREA)
- General Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Optics & Photonics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Particle Accelerators (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
Description
Yb2O3/TREO (% min.) | 99.9 | ||
TREO (% min.) | 99 | ||
Loss On Ignition (% max.) | 1 | ||
% max. | |||
Rare Earth Impurities | |||
Tb4O7/TREO | 0.001 | ||
Dy2O3/TREO | 0.001 | ||
Ho2O3/TREO | 0.001 | ||
Er2O3/TREO | 0.01 | ||
Tm2O3/TREO | 0.01 | ||
Lu2O3/TREO | 0.001 | ||
Y2O3/TREO | 0.001 | ||
Non-Rare Earth Impurities | |||
Fe2O3 | 0.001 | ||
SiO2 | 0.01 | ||
CaO | 0.01 | ||
Cl− | 0.03 | ||
NiO | 0.001 | ||
ZnO | 0.001 | ||
PbO | 0.001 | ||
176 Yb(n,γ)177 Yb(−,β)177 Lu.
Claims (24)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2015/051844 WO2016119864A1 (en) | 2015-01-29 | 2015-01-29 | Method of preparing irradiation targets for radioisotope production and irradiation target |
Publications (2)
Publication Number | Publication Date |
---|---|
US20180019032A1 US20180019032A1 (en) | 2018-01-18 |
US10714224B2 true US10714224B2 (en) | 2020-07-14 |
Family
ID=52434817
Family Applications (1)
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US15/545,807 Active 2035-05-25 US10714224B2 (en) | 2015-01-29 | 2015-01-29 | Method of preparing of irradiation targets for radioisotope production and irradiation target |
Country Status (9)
Country | Link |
---|---|
US (1) | US10714224B2 (en) |
EP (1) | EP3251124B1 (en) |
KR (1) | KR102319891B1 (en) |
CN (1) | CN107210076B (en) |
CA (1) | CA2973623C (en) |
ES (1) | ES2718949T3 (en) |
PL (1) | PL3251124T3 (en) |
RU (1) | RU2682666C2 (en) |
WO (1) | WO2016119864A1 (en) |
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DE102017125606A1 (en) | 2017-11-02 | 2019-05-02 | Kernkraftwerk Gösgen-Däniken Ag | Valve block for a piggable and / or solid-conducting line system and distribution line system |
CN111440000B (en) * | 2020-04-24 | 2022-04-29 | 河北恒博新材料科技股份有限公司 | Preparation method of large-size rotary ceramic target |
Citations (11)
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CN1159198A (en) | 1994-09-09 | 1997-09-10 | 帝国化学工业澳大利亚经营有限公司 | Polymer beads and method for preparation thereof |
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US20040254418A1 (en) * | 2003-06-10 | 2004-12-16 | Munro John J. | X-ray and gamma ray emitting temporary high dose rate brachytherapy source |
CN1938115A (en) | 2004-06-30 | 2007-03-28 | Tdk株式会社 | Method for producing raw material powder for rare earth sintered magnet, method for producing rare earth sintered magnet, granule and sintered article |
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EP2093773A2 (en) | 2008-02-21 | 2009-08-26 | GE-Hitachi Nuclear Energy Americas LLC | Apparatus and methods for production of radioisotopes in nuclear reactor instrumentation tubes |
CN101628811A (en) | 2009-08-14 | 2010-01-20 | 中国科学院上海光学精密机械研究所 | Transparent ceramic and preparation method thereof |
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CN104043138A (en) | 2014-05-29 | 2014-09-17 | 北京大学 | Rare earth-based nanoparticle magnetic resonance contrast agent and preparation method thereof |
Family Cites Families (1)
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US6381504B1 (en) * | 1996-05-06 | 2002-04-30 | Pavilion Technologies, Inc. | Method for optimizing a plant with multiple inputs |
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2015
- 2015-01-29 ES ES15701798T patent/ES2718949T3/en active Active
- 2015-01-29 US US15/545,807 patent/US10714224B2/en active Active
- 2015-01-29 CN CN201580074837.3A patent/CN107210076B/en active Active
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KR102319891B1 (en) | 2021-11-02 |
CA2973623A1 (en) | 2016-08-04 |
RU2017130345A3 (en) | 2019-02-28 |
WO2016119864A1 (en) | 2016-08-04 |
PL3251124T3 (en) | 2019-06-28 |
US20180019032A1 (en) | 2018-01-18 |
KR20170108130A (en) | 2017-09-26 |
RU2682666C2 (en) | 2019-03-20 |
ES2718949T3 (en) | 2019-07-05 |
RU2017130345A (en) | 2019-02-28 |
CA2973623C (en) | 2023-03-28 |
CN107210076B (en) | 2019-06-28 |
CN107210076A (en) | 2017-09-26 |
EP3251124A1 (en) | 2017-12-06 |
EP3251124B1 (en) | 2019-01-09 |
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